Have questions? Visit https://www.reddit.com/r/SNPedia

rs1047016803

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1047016803(C;T)
Make rs1047016803(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position57651502
GeneADGRG1
is asnp
is mentioned by
dbSNPrs1047016803
dbSNP (old)rs1047016803
ClinGenrs1047016803
ebirs1047016803
HLIrs1047016803
Exacrs1047016803
Gnomadrs1047016803
Varsomers1047016803
Maprs1047016803
PheGenIrs1047016803
Biobankrs1047016803
1000 genomesrs1047016803
hgdprs1047016803
ensemblrs1047016803
gopubmedrs1047016803
geneviewrs1047016803
scholarrs1047016803
googlers1047016803
pharmgkbrs1047016803
gwascentralrs1047016803
openSNPrs1047016803
23andMers1047016803
23andMe allrs1047016803
SNPshotrs1047016803
SNPdbers1047016803
MSV3drs1047016803
GWAS Ctlgrs1047016803
Max Magnitude0
ClinVar
Risk rs1047016803(T;T)
Alt rs1047016803(T;T)
Reference Rs1047016803(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADGRG1 GPR56
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.57685414C>T
CLNSRC
CLNACC RCV000434335.1,